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A comprehensive tandem repeat catalog of the human genome.
Chiu, Readman; Rajan-Babu, Indhu-Shree; Friedman, Jan M; Birol, Inanc.
Afiliação
  • Chiu R; Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, BC V5Z 4S6, Canada.
  • Rajan-Babu IS; Department of Medical Genetics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.
  • Friedman JM; Department of Medical Genetics, University of British Columbia, Vancouver, BC V5Z 4H4, Canada.
  • Birol I; BC Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.
medRxiv ; 2024 Jun 20.
Article em En | MEDLINE | ID: mdl-38947075
ABSTRACT
With the increasing availability of long-read sequencing data, high-quality human genome assemblies, and software for fully characterizing tandem repeats, genome-wide genotyping of tandem repeat loci on a population scale becomes more feasible. Such efforts not only expand our knowledge of the tandem repeat landscape in the human genome but also enhance our ability to differentiate pathogenic tandem repeat mutations from benign polymorphisms. To this end, we analyzed 272 genomes assembled using datasets from three public initiatives that employed different long-read sequencing technologies. Here, we report a catalog of over 18 million tandem repeat loci, many of which were previously unannotated. Some of these loci are highly polymorphic, and many of them reside within coding sequences.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: MedRxiv Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá
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